grant

Discovery and anti-tumor activity of the first antagonists targeting human Sonic Hedgehog autoprocessing

Organization STATE UNIVERSITY OF NY,BINGHAMTONLocation BINGHAMTON, UNITED STATESPosted 6 Mar 2024Deadline 28 Feb 2027
NIHUS FederalResearch GrantFY202521+ years oldAddressAdultAdult HumanAnabolismApoptosisApoptosis PathwayAssayBindingBioassayBiological AssayBioluminescenceCancersCell BodyCell Communication and SignalingCell Growth in NumberCell LineCell Membrane PermeabilityCell MultiplicationCell ProliferationCell SignalingCell secretionCellLineCellsCellular AssayCellular ProliferationCellular SecretionChemoresistanceCholesterolCircadian RhythmsClinicalCollaborationsColon CancerColon CarcinomaCouplesDrosophilaDrosophila genusDrug TargetingDrug resistanceDrugsEmbryo DevelopmentEmbryogenesisEmbryonic DevelopmentEnzyme GeneEnzymesErinaceidaeEventExhibitsGeneHomologGeneralized GrowthGoalsGrowthHedgehog (Hh) signal transduction pathwayHedgehogsHigh Throughput AssayHomologHomologous GeneHomologueHumanIn VitroIntracellular Communication and SignalingLeftLettersLibrariesLigandsMalignant CellMalignant NeoplasmsMalignant TumorMedicationModern ManMolecularMolecular InteractionMultiple MyelomaNCATSNational Center for Advancing Translational SciencesNational Institutes of HealthNyctohemeral RhythmOncogenicPermeabilityPharmaceutical PreparationsPhotoaffinity LabelsPlasma-Cell MyelomaPositionPositioning AttributeProgrammed Cell DeathProtein FamilyProteinsReactionReceptor ProteinReporterReportingSHHSHH geneSignal TransductionSignal Transduction SystemsSignalingSonic HedgehogSpecificityStrains Cell LinesSystemTestingTherapeuticTissue GrowthTranslationsTumor CellTwenty-Four Hour RhythmUnited States National Institutes of HealthUniversitiesWorkadulthoodantagonismantagonistanti-canceranti-cancer therapeuticanti-tumor effectanticancer activityantitumor effectbiological signal transductionbiosynthesiscancer cellcancer in the coloncell assaychemoresistantchemotherapy resistancechemotherapy resistantcircadian processcircadian rhythmicitycultured cell linedaily biorhythmdeprivationdrug resistantdrug/agentextracellularfruit flyhedgehog signalinghedgehog signaling pathwayhh signaling pathwayhigh riskhigh throughput screeninginhibitorinnovateinnovationinnovativemalignancymembrane permeabilityminiaturizeminiaturizedmyelomamyelomatosisneoplasm/cancerneoplastic cellnovelontogenypre-clinical evaluationpreclinical evaluationprogenitor cell maintenanceprogenitor maintenancereceptorresistance to Drugresistant to Drugscreeningscreeningssmall moleculesmoothened signaling pathwaystem cell maintenancesuccesssynergismtargeted cancer therapytranslationtumortumorigenicvalidation studies
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Full Description

ABSTRACT
We are pursuing the first anti-tumor small molecules that act specifically against human Sonic Hh protein

autoprocessing, a unique biosynthetic event that is necessary to drive oncogenic hedgehog (Hh) ligand

dependent cell/cell signaling. Sonic Hh protein autoprocessing involves a precursor form of Hh and is

responsible for liberating the mature Sonic Hh signaling ligand while also modifying the ligand’s terminal

carboxyl group with cholesterol. The long-standing challenge has been to discover small molecules that

specifically antagonize this key reaction within the tumor cell. To facilitate discovery, we have devised the

first in-cell assay system to screen for antagonists of human Hh autoprocessing at high throughput. Our

assay couples intracellular Sonic Hh autoprocessing to the extracellular secretion of a bioluminescent

reporter enzyme. We recently miniaturized this assay for 1536-well plates and in preliminary work,

completed a successful pilot screen against LOPAC. Here we propose a two-year high risk/gain strategy

that integrates: (AIM 1) In-cell quantitative high throughput screening in collaboration with the National

Center for Advancing Translational Science (NCATS) to discover the first bioactive drug-like antagonists

of human Sonic Hh autoprocessing; (AIM 2) Pre-clinical evaluation of the anti-tumor effects of those novel

Hh autoprocessing inhibitors toward human multiple myeloma and human colon cancer cells, which exhibit

Hh-ligand dependent growth. We hypothesize that specific antagonists of Sonic Hh autoprocessing will

deplete extracellular Sonic Hh ligand. Tumor apoptosis is the expected result of this ligand deprivation

strategy. In summary, using an innovative assay and novel anti-Hh approach, we are poised to address a

significant gap in the field of Hh signaling while pursuing a new class of cancer therapeutics.

Grant Number: 5R21CA282857-02
NIH Institute/Center: NIH

Principal Investigator: Brian Callahan

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